Canonical Allele Identifier: PA2828413243
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405973
ClinVar RCV Id: RCV000464873 RCV000569892 RCV001721496 RCV004533160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ser1052Phe
CA045537
NM_001370404.1:c.3155C>T